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Found 4 matching solutions for this experiment
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The second dimension was run until the fragment of interest had migrated ∼10 cm. For long-range 2D AGEs, 5 μg of mitochondrial nucleic acids was digested with FastDigest BamHI or PvuII (Thermo Scientific), which cut mtDNA only once, and run on a 0.28% agarose gel in 1× TBE until the linearized mtDNA fragment had migrated 10 cm into the gel. |
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Protocol tips |
The second dimension was run until the fragment of interest had migrated ∼10 cm. For long-range 2D AGEs, 5 μg of mitochondrial nucleic acids was digested with FastDigest BamHI or PvuII (Thermo Scientific), which cut mtDNA only once, and run on a 0.28% agarose gel in 1× TBE until the linearized mtDNA fragment had migrated 10 cm into the gel. |
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Digest a high copy number plasmid backbone (see materials) with PvuII-HF and PstI-HF at 37 °C for 1 hr (see Table 5) according to the manufacturer’s protocol. PvuII-HF and PstI-HF are high fidelity restriction enzymes, which dramatically reduce unspecific cuts. |
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Digest a high copy number plasmid backbone (see materials) with PvuII-HF and PstI-HF at 37 °C for 1 hr (see Table 5) according to the manufacturer’s protocol. PvuII-HF and PstI-HF are high fidelity restriction enzymes, which dramatically reduce unspecific cuts. |
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Enzymes were used at a maximum concentration compatible with glycerol content lower than 4.75%. MvaI, HindIII, PvuII (Fastdigest™ series) and BcnI enzymes were from Thermo Scientific™. AvaII, HinP1I and EcoRV were from New England Biolabs. |
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Enzymes were used at a maximum concentration compatible with glycerol content lower than 4.75%. MvaI, HindIII, PvuII (Fastdigest™ series) and BcnI enzymes were from Thermo Scientific™. AvaII, HinP1I and EcoRV were from New England Biolabs. |
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First, the Tet gene of pBR322 (Invitrogen) was removed by HindIII/PvuII (NEB) double digestion, followed by insertion of the linker, 5′-AGCTTAGATCTTGATCAGGATCCCAG-3′, which contains BglII and BamHI sites, to create pBR-Linker. |
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First, the Tet gene of pBR322 (Invitrogen) was removed by HindIII/PvuII (NEB) double digestion, followed by insertion of the linker, 5′-AGCTTAGATCTTGATCAGGATCCCAG-3′, which contains BglII and BamHI sites, to create pBR-Linker. |
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